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Scientific Articles - PTR-MS Bibliography

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Publications

Found 7 results
Title [ Year(Asc)]
Filters: Author is Lelieveld, J  [Clear All Filters]
2010
[Holzinger2010] Holzinger, R., J. Williams, F. Herrmann, J. Lelieveld, NM. Donahue, and T. Roeckmann, "Aerosol analysis using a Thermal-Desorption Proton-Transfer-Reaction Mass Spectrometer (TD-PTR-MS): a new approach to study processing of organic aerosols", Atmospheric chemistry and physics, vol. 10, no. 5: Copernicus Publications, pp. 2257–2267, 2010.
Link: http://igitur-archive.library.uu.nl/phys/2011-0323-200410/UUindex.html
Abstract
We present a novel analytical approach to measure the chemical composition of organic aerosol. The new instrument combines proton-transfer-reaction mass-spectrometry (PTR-MS) with a collection-thermal-desorption aerosol sampling technique. For secondary organic aerosol produced from the reaction of ozone with isoprenoids in a laboratory reactor, the TD-PTR-MS instrument detected typically 80% of the mass that was measured with a scanning mobility particle sizer (SMPS). The first field deployment of the instrument was the EUCAARI-IOP campaign at the CESAR tall tower site in the Netherlands. For masses with low background values (∼30% of all masses) the detection limit of aerosol compounds was below 0.2 ng/m3 which corresponds to a sampled compound mass of 35 pg. Comparison of thermograms from ambient samples and from chamber-derived secondary organic aerosol shows that, in general, organic compounds from ambient aerosol samples desorb at much higher temperatures than chamber samples. This suggests that chamber aerosol is not a good surrogate for ambient aerosol and therefore caution is advised when extrapolating results from chamber experiments to ambient conditions
[Sinha2010] Sinha, V., J. Williams, J. Lelieveld, TM. Ruuskanen, MK. Kajos, J. Patokoski, H. Hellen, H. Hakola, D. Mogensen, M. Boy, et al., "OH reactivity measurements within a boreal forest: evidence for unknown reactive emissions", Environmental science & technology, vol. 44, no. 17: ACS Publications, pp. 6614–6620, 2010.
Link: http://pubs.acs.org/doi/abs/10.1021/es101780b
Abstract
Boreal forests emit large amounts of volatile organic compounds (VOCs) which react with the hydroxyl radical (OH) to influence regional ozone levels and form secondary organic aerosol. Using OH reactivity measurements within a boreal forest in Finland, we investigated the budget of reactive VOCs. OH reactivity was measured using the comparative reactivity method, whereas 30 individual VOCs were measured using proton transfer reaction mass spectrometry, thermal-desorption gas chromatography mass spectrometry, and liquid chromatography mass spectrometry, in August 2008. The measured OH reactivity ranged from below detection limit (3.5 s−1), to 60 s−1 in a single pollution event. The average OH reactivity was 9 s−1 and no diel variation was observed in the profiles. The measured OH sinks (30 species) accounted for only 50% of the total measured OH reactivity, implying unknown reactive VOCs within the forest. The five highest measured OH sinks were: monoterpenes (1 s−1), CO (0.7 s−1), isoprene (0.5 s−1), propanal and acetone (0.3 s−1), and methane (0.3 s−1). We suggest that models be constrained by direct OH reactivity measurements to accurately assess the impact of boreal forest emissions on regional atmospheric chemistry and climate.
2008
[Sinha2008] Sinha, V., J. Williams, JN. Crowley, and J. Lelieveld, "The Comparative Reactivity Method–a new tool to measure total OH Reactivity in ambient air", Atmospheric Chemistry and Physics, vol. 8, no. 8: Copernicus GmbH, pp. 2213–2227, 2008.
Link: http://www.atmos-chem-phys.net/8/2213/2008/acp-8-2213-2008.pdf
2005
[Reus2005] de Reus, M., H. Fischer, R. Sander, V. Gros, R. Kormann, G. Salisbury, R. Van Dingenen, J. Williams, M. Zöllner, and J. Lelieveld, "Observations and model calculations of trace gas scavenging in a dense Saharan dust plume during MINATROC", Atmospheric Chemistry and Physics, vol. 5, no. 7: Copernicus GmbH, pp. 1787–1803, 2005.
Link: http://www.atmos-chem-phys.net/5/1787/
2003
[Gros2003] Gros, V., J. Williams, JA. van Aardenne, G. Salisbury, R. Hofmann, MG. Lawrence, R. von Kuhlmann, J. Lelieveld, M. Krol, H. Berresheim, et al., "Origin of anthropogenic hydrocarbons and halocarbons measured in the summertime European outflow (on Crete in 2001)", Atmospheric Chemistry and Physics, vol. 3, no. 4: Copernicus GmbH, pp. 1223–1235, 2003.
Link: http://www.atmos-chem-phys.net/3/1223/2003/acp-3-1223-2003.pdf
2001
[Williams2001] Williams, J., U. Poeschl, PJ. Crutzen, A. Hansel, R. Holzinger, C. Warneke, W. Lindinger, and J. Lelieveld, "An atmospheric chemistry interpretation of mass scans obtained from a proton transfer mass spectrometer flown over the tropical rainforest of Surinam", Journal of atmospheric chemistry, vol. 38, no. 2: Springer, pp. 133–166, 2001.
Link: http://www.springerlink.com/index/v26n6440307112k1.pdf
[Laat2001] de Laat, ATJ., JA. de Gouw, J. Lelieveld, and A. Hansel, "Model analysis of trace gas measurements and pollution impact during INDOEX", Journal of Geophysical Research: Atmospheres (1984–2012), vol. 106, no. D22: Wiley Online Library, pp. 28469–28480, 2001.
Link: http://adsabs.harvard.edu/abs/2001JGR...10628469D
Abstract
An analysis of acetone (CH3COCH3) and acetonitrile (CH3CN) measurements, performed during the Indian Ocean Experiment (INDOEX), using a chemistry general circulation model is presented. A comparison with measurements indicates that the model simulates realistic CO and acetone distributions, except toward the Indian west coast near the surface. The latter may be related to a sea breeze circulation at the Indian west coast, which is not resolved by the model. A comparison of the measured and modeled correlation between CO and acetone indicates the presence of a background marine acetone source. A model sensitivity study suggests a global marine emission strength of 15-20 Tg acetone yr-1, which is a significant contribution to the estimated global acetone source of 56 (37-80) Tg acetone yr-1. The comparison of measured and modeled CO-acetonitrile correlation from surface measurements indicates that a model sink of acetonitrile in the marine boundary layer is missing. A model sensitivity study suggests that this could be dry deposition (deposition velocity estimate: 0.01-0.05 cms-1) on the ocean surface. A comparison of measured and modeled tropospheric acetonitrile indicates that the model overestimates the free tropospheric acetonitrile mixing ratios up to a factor of 3, which points to a missing free tropospheric sink of acetonitrile in the model. A possible explanation may be stratospheric loss and subsequent stratosphere-troposphere exchange, which was not included in the model.

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Download Contributions to the International Conference on Proton Transfer Reaction Mass Spectrometry and Its Applications:

 

Selected PTR-MS related Reviews

F. Biasioli, C. Yeretzian, F. Gasperi, T. D. Märk: PTR-MS monitoring of VOCs and BVOCs in food science and technology, Trends in Analytical Chemistry 30 (7) (2011).
Link

J. de Gouw, C. Warneke, T. Karl, G. Eerdekens, C. van der Veen, R. Fall: Measurement of Volatile Organic Compounds in the Earth's Atmosphere using Proton-Transfer-Reaction Mass Spectrometry. Mass Spectrometry Reviews, 26 (2007), 223-257.
Link

W. Lindinger, A. Hansel, A. Jordan: Proton-transfer-reaction mass spectrometry (PTR–MS): on-line monitoring of volatile organic compounds at pptv levels, Chem. Soc. Rev. 27 (1998), 347-375.
Link

 

Lists with PTR-MS relevant publications of the University of Innsbruck can be found here: Atmospheric and indoor air chemistry, IMR, Environmental Physics and Nano-Bio-Physics

 

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